(Q32143975)
English
congenital stationary night blindness autosomal dominant 1
A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in mutations in the RHO gene on chromosome 3q22.1.
- rhodopsin-related congenital stationary night blindness
- CSNBAD1
- NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1
- congenital stationary night blindness autosomal dominant type 1
- Night Blindness, Congenital Stationary, Autosomal Dominant type 1
- Night Blindness, Congenital Stationary, Rhodopsin-Related
- NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1
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Identifiers
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